scholarly journals Regulating Direct-to-Consumer Drug Information: A Case Study of Eli Lilly’s Canadian 40over40 Erectile Dysfunction Campaign

2015 ◽  
Vol 10 (4) ◽  
pp. 16-22 ◽  
Author(s):  
Jean-Christophe Bélisle Pipon ◽  
Bryn Williams-Jones
2021 ◽  
Vol 9 (1) ◽  
pp. 100289
Author(s):  
Joel J. Wackerbarth ◽  
Richard J. Fantus ◽  
Annie Darves-Bornoz ◽  
Marah C. Hehemann ◽  
Brian T. Helfand ◽  
...  

2018 ◽  
Vol 2 (2) ◽  
Author(s):  
Janelle Applequist

Pfizer, manufacturer of the erectile dysfunction prescription treatment Viagra, has been a staple in the pharmaceutical advertising arena since broadcast versions of such ads became legally permissible in the United States in 1997. Given that the patent for Viagra is soon set to expire, it is important that research take a look back in an attempt to contextualize the brand’s place in shaping medicinal marketing culture. Of particular interest is the period beginning in 2014, when Viagra’s most unconventional campaign yet began using a tactic that was the first of its kind for the pharmaceutical industry. By removing the actual consumer of the medication from these ads (males), Viagra has paved the way for pharmaceutical advertising to target the medicinal partner. This manuscript reviews the first use of the medicinal partner in the pharmaceutical advertising sector, conducting a textual analysis of Viagra’s use of this mediated relationship. The medicinal partner is the pharmaceutical industry’s attempt to target a patient’s social circle in an effort to promote a discourse that suggests a medicinal remedy for a problem. This analysis describes how social meaning and relationships underlie the market transaction of obtaining a prescription, as has been previously established through the processes of medicalization and pharmaceutical fetishism. These advertisements create belief in the larger sense, meaning Pfizer is infiltrating upon the patient’s process of choice and consumption of medicinal remedies. Viagra is simultaneously encouraging male consumers to celebrate the brand while using female ambassadors to influence the decision to request medicinal intervention.


2017 ◽  
Vol 14 (5) ◽  
pp. e340-e341
Author(s):  
Pavel Turcan ◽  
Pavel Pokorny ◽  
Martin Prochazka ◽  
Jana Kvintova ◽  
Martin Sigmund
Keyword(s):  

2016 ◽  
Vol 3 (1) ◽  
pp. 74-94 ◽  
Author(s):  
Maria-Cornelia Wermuth

Although localization is, in the first place, related to the cultural adaptation and translation of software and websites, it is important for written materials as well. In this paper we investigate how specialized medical discourse used in the Summary of Product Characteristics (SmPC) is localized in patient leaflets (PL). Both documents are issued by the European Medicines Agency (EMA) and provide detailed information on the product compiled and distributed by the drug manufacturer, after EMA review and approval. We describe by means of a case study the formal and linguistic features of SmPCs and PLs and we investigate how the specialized source text is localized in its patient-friendly version. The aim of this investigation is to increase awareness and understanding of localization strategies adopted on the intralingual level in the communication of scientific-medical knowledge to a non-expert audience.


Urology ◽  
2020 ◽  
Vol 143 ◽  
pp. 165-172 ◽  
Author(s):  
Robert H. Shahinyan ◽  
Arash Amighi ◽  
Alson N. Carey ◽  
Dar A. Yoffe ◽  
Devyn C. Hodge ◽  
...  

2020 ◽  
Vol 17 (1) ◽  
pp. S27-S28
Author(s):  
R. Shahinyan ◽  
A. Amighi ◽  
A. Carey ◽  
D. Yoffe ◽  
M. Pollard ◽  
...  

2019 ◽  
Vol 44 (5) ◽  
pp. 765-787
Author(s):  
Denis G. Arnold ◽  
James L. Oakley

Abstract Context: Spending on direct-to-consumer advertising (DTCA) for prescription pharmaceuticals has risen to record levels, five times as much as in 1996 in inflation-adjusted dollars. Major health care provider organizations have called for additional regulation of DTCA. These organizations argue that the negative impact of such advertising outweighs the informational value claimed by the pharmaceutical industry. The industry maintains that further restrictions on DTCA are not warranted because it is successfully self-regulating via “guiding principles” for DTCA as certified by firm executives. Methods: The authors measured recent industry spending on DTCA and used regression models of Nielsen Monitor-Plus data to assess pharmaceutical firm self-regulation after the public disclosure of noncompliance with industry self-regulatory principles, specifically regarding the exposure of children and adolescents to broadcast advertisements for erectile dysfunction drugs. Findings: Public disclosure of noncompliance with self-regulatory DTCA standards did not bring advertising into compliance. Results demonstrate that firms failed to meet the industry standard during every quarter of the six-year period of this study. Conclusions: Results support previous research findings that pharmaceutical self-regulation is a deceptive blocking strategy rather than a means for the industry to police itself. Policy recommendations include broadcast restrictions on adult content and deincentivizing DTCA via tax reform.


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